510(k) K062959 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)
DMS 300-2, 300-3 AND 300-4
| Applicant | Diagnostic Monitoring Software, Stateline NV, US |
| Decision | Substantially Equivalent, Oct 16, 2006 |
| Received | Sep 29, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062959
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.